EP0261885A1 - Glaszusammensetzungen - Google Patents

Glaszusammensetzungen Download PDF

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Publication number
EP0261885A1
EP0261885A1 EP87308279A EP87308279A EP0261885A1 EP 0261885 A1 EP0261885 A1 EP 0261885A1 EP 87308279 A EP87308279 A EP 87308279A EP 87308279 A EP87308279 A EP 87308279A EP 0261885 A1 EP0261885 A1 EP 0261885A1
Authority
EP
European Patent Office
Prior art keywords
weight
glass composition
borosilicate glass
amount
composition according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP87308279A
Other languages
English (en)
French (fr)
Other versions
EP0261885B1 (de
Inventor
Brian Yale
Kenneth Melvin Fyles
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pilkington Group Ltd
Original Assignee
Pilkington PLC
Pilkington Brothers Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pilkington PLC, Pilkington Brothers Ltd filed Critical Pilkington PLC
Publication of EP0261885A1 publication Critical patent/EP0261885A1/de
Application granted granted Critical
Publication of EP0261885B1 publication Critical patent/EP0261885B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/11Glass compositions containing silica with 40% to 90% silica, by weight containing halogen or nitrogen
    • C03C3/112Glass compositions containing silica with 40% to 90% silica, by weight containing halogen or nitrogen containing fluorine
    • C03C3/115Glass compositions containing silica with 40% to 90% silica, by weight containing halogen or nitrogen containing fluorine containing boron
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C4/00Compositions for glass with special properties
    • C03C4/08Compositions for glass with special properties for glass selectively absorbing radiation of specified wave lengths
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/095Glass compositions containing silica with 40% to 90% silica, by weight containing rare earths
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L31/00Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
    • H01L31/04Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
    • H01L31/042PV modules or arrays of single PV cells
    • H01L31/048Encapsulation of modules
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S501/00Compositions: ceramic
    • Y10S501/90Optical glass, e.g. silent on refractive index and/or ABBE number
    • Y10S501/905Ultraviolet transmitting or absorbing

Definitions

  • the present invention relates to borosilicate glass compositions. More particularly, the invention relates to borosilicate glass compositions which incorporate cerium oxide and which are suitable for use as protective covers for solar cells, especially solar cells used in satellites.
  • Glass compositions which are intended for use as protective covers for solar cells must have a number of optical characteristics. Such glass compositions must, inter alia, exhibit the following properties:
  • Borosilicate glasses are found to have coefficients of linear expansion which are of the desired value.
  • cerium oxide tends to induce phase separation in the glass and also tends to impart a yellow to brown colouration in the glass thereby impairing the high white light transmission of the glass.
  • the present invention aims to overcome these drawbacks by providing a class of borosilicate glass compositions which contain 2.0% by weight or more of CeO2, in the presence of antimony oxide and/or arsenic oxide.
  • the present invention provides a low alkali borosilicate glass composition
  • a low alkali borosilicate glass composition comprising 60 to 78% by weight of SiO2 10 to 25% by weight of B2O3 3.5 to 6.0% by weight of R2O, wherein R2O represents Na2O, K2O and/or Li2O, 2.0 to 6.5% by weight of CeO2, and 0.25 to 8.0% by weight of Sb2O3 and/or As2O3, the percentages being based on the total weight of the glass composition.
  • Cerium oxide (ceria) is necessary to impart the required UV absorption and radiation stability to the borosilicate glass compositions. Ceria is always expressed as ceric or cerium 4 oxide, even though it is generally present in the glass as a mixture of ceric and cerous (cerium 3) oxides, and may even be present wholly as cerium 3 oxide.
  • cerium oxides It is difficult to incorporate large quantities of cerium oxides into low-alkali borosilicate glass compositions owing to the tendency of cerium to promote phase separation, and the maximum cerium levels can only be used with boric oxide levels below about fifteen percent. Cerium oxides also tend to impart a yellow to brown colouration to known borosilicate glass compositions, and it is difficult to combine the maximum UV absorption with good white light transmission. For example, if ceric oxide is added to a typical commercial low-expansion borosilicate glass of the type known as Pyrex, then the glass becomes darkly coloured with cerium oxide contents exceeding about two percent and the glasses will be unsuitable for use as solar cell covers.
  • the quantity of cerium oxide can be increased above 2% by weight if the glass composition incorporates Sb2O3 and/or As2O3 in a total amount of from 0.25 to 8.0% by weight.
  • the amount of Sb2O3 is from 0 to 2.5% by weight, and the amount of As2O3 is from 0 to 2.5% by weight.
  • Antimony and/or arsenic oxides have been found to have a marked effect on the colour of borosilicate glass compositions containing cerium. The antimony and arsenic oxides increase the transmission of the borosilicate glass in the visible part of the spectrum and allow the desired combination of good white light transmission, low ultra-violet light transmission and high radiation stability to be obtained.
  • Titanium dioxide in combination with cerium oxide serves to reduce the UV transmission of the glasses and to reduce the tendency of the glasses to darken when exposed to radiation (i.e. it increases the radiation stability of the glass). Incorporation of titanium dioxide in the glass compositions thus makes it possible to use lower cerium levels than would otherwise be necessary. Furthermore, titanium dioxide also reduces melt viscosity more than does cerium oxide, and the presence of titanium dioxide improves melting and refining. However, titanium dioxide also increases visible absorption and this restricts the amount which may be included in the borosilicate glass compositions of the invention.
  • the glass compositions comprise up to 2.0% by weight TiO2.
  • the amount of TiO2 ranges from 0.25 to 2.0% by weight, and the total amount of TiO2 + CeO2 in the glass composition ranges from 3.5 to 7.0% by weight.
  • Alumina helps to improve the chemical durability of the glass composition and helps to inhibit phase separation, but it increases liquidus temperatures, and also darkens the colour of the glasses.
  • Zirconia also improves chemical durability, and does not darken the colour as much as alumina, but increases liquidus temperature more than does alumina.
  • the glass compositions of the invention comprise up to 3% by weight of Al2O3 + ZrO2.
  • the amount of Al2O3 ranges from 0.5 to 3% by weight and the amount of ZrO2 ranges from 0 to 2% by weight.
  • B2O3 Boric oxide (B2O3) contents below 10% by weight lead to melting and refining difficulties. Melting and refining of the glass composition improve as boric oxide levels increase, but phase separation can occur if maximum cerium levels coincide with maximum boron levels.
  • the total amount of the oxides of lithium, sodium and potassium (defined as R2O above) must be limited to about 6.0% by weight to keep the coefficient of linear thermal expansion of the borosilicate glass close to that of silicon.
  • the optimum amount has been found to be approximately 4.5%.
  • the minimum amount of R2O is at approximately 3.5% total but melting of the glass components becomes more difficult as alkali levels fall and there is no advantage in seeking to minimise alkali contents.
  • the individual alkali metal oxides have different properties. Lithium oxide is the most effective in promoting melting and refining, and also gives good white light transmission, but the tendency to phase separate is aggravated and lithium oxide must not exceed about 1.5% by weight of the glass. Potassium oxide is the least effective in promoting melting and refining and gives darker glasses, but phase separation is minimised. Sodium oxide occupies an intermediate position. A mixture of all three alkali metal oxides offers advantages. If lithium oxide is present above 1% then the maximum sodium oxide level is approximately 3% in order to avoid phase separation.
  • Preferred conte nts of the alkali metal oxides are as follows: Li2O 0 to 1.5 % by weight Na2O 0 to 5.5 % by weight K2O 0 to 5.5 % by weight
  • zinc oxide and/or alkaline earth metal oxides such as MgO, BaO, CaO and SrO may be added to the batch of glass forming components. These materials are of value in reducing the viscosity of the glass melt when such reduction is required.
  • the amount of ZnO added to the batch can be up to 5% by weight; the amount of alkaline earth metal oxides can be up to 5% by weight.
  • the borosilicate glass compositions of the invention are prepared using conventional procedures for the preparation of borosilicate glasses. Accordingly specific details of the preparation of the glass compositions are not given herein since a person skilled in the art will readily be able to determine the appropriate processing conditions for preparing the borosilicate glass compositions.
  • the low alkali borosilicate glass compositions of the invention provide the desired optical characteristics of good white light transmission, high ultra-violet light absorption and good radiation stability which are required for a glass composition which is to be used as a protective cover for a solar cell.
  • a further advantage of the glass compositions of the invention is that the glass compositions are suitable for the manufacture of thin micro-sheet having a thickness of about 50 to 300 microns which is desirable for glass which is to be used as a protective cover for solar cells.
  • the present glass compositions also have a coefficient of linear expansion close to that of silicon and possess the added characteristic that they can readily be sealed to a silicon surface.
  • the present borosilicate glass compositions readily lend themselves to pretreatments such as cleaning, etching and coating.
  • many known borosilicate glass compositions are not suitable for such pretreatments since they have poor chemical durability and a tendency to undergo phase separation if subjected to the said pretreatments.
  • Examples in the accompanying Table broadly illustrate the glass compositions of the invention.
  • Examples numbers 1, 2, 3, 4, 8, 14, 16, 18 and 26 have been tested for radiation stability by exposing polished samples, thickness between 100 microns and 200 microns, to 5.7 ⁇ 1015 1 MEV electrons in vacuum ( ⁇ 1 ⁇ 10 ⁇ 3 torr) and measuring the loss in visible light transmission. Transmission losses ranged from 1.5% to 4.0% between 400 and 450 nm, which is regarded as satisfactory.
  • the thickness of covers for solar cells can range from 50 microns to 300 microns; it is possible for many formulations of glass compositions within the scope of the present invention to be suitable for producing thin glass sheets but unsuitable for producing thick glass sheets, and vice versa .
  • the total amount of CeO2 plus TiO2 needs to be high, typically greater than five percent, to give the required UV absorption.
  • many of these compositions will be coloured too darkly to be suitable for the thicker covers.
  • These high UV absorbing glasses may be bleached to some extent by increasing antimony concentrations to above one percent, but maximum levels of CeO2 + TiO2 (ceria plus titania) are not necessary for the thicker covers (i.e. above about 150 microns in thickness) and it would therefore also be possible to use CeO2 + TiO2 levels below five percent in these cases.
EP87308279A 1986-09-26 1987-09-18 Glaszusammensetzungen Expired - Lifetime EP0261885B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8623214 1986-09-26
GB868623214A GB8623214D0 (en) 1986-09-26 1986-09-26 Glass compositions

Publications (2)

Publication Number Publication Date
EP0261885A1 true EP0261885A1 (de) 1988-03-30
EP0261885B1 EP0261885B1 (de) 1991-01-23

Family

ID=10604853

Family Applications (1)

Application Number Title Priority Date Filing Date
EP87308279A Expired - Lifetime EP0261885B1 (de) 1986-09-26 1987-09-18 Glaszusammensetzungen

Country Status (6)

Country Link
US (1) US5017521A (de)
EP (1) EP0261885B1 (de)
JP (1) JPH07100616B2 (de)
KR (1) KR950006200B1 (de)
DE (1) DE3767633D1 (de)
GB (1) GB8623214D0 (de)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0505061A2 (de) * 1991-03-22 1992-09-23 Pilkington Plc Borosilicatglaszusammensetzung
EP0779252A1 (de) 1995-12-08 1997-06-18 Pilkington Plc Strahlungsbeständiges Glas und Glasgegenstände
EP1026130A1 (de) * 1999-02-05 2000-08-09 Corning Incorporated Glas für Abdeckung von Sonnenzellen
EP1059674A2 (de) * 1999-06-09 2000-12-13 Sharp Kabushiki Kaisha Abgedeckte Solarzelle und Herstellungsverfahren
US6262358B1 (en) * 1999-02-18 2001-07-17 Sharp Kabushiki Kaisha Solar cell module and solar cell panel using the same
EP1798775A2 (de) * 2005-12-17 2007-06-20 Solarwatt Ag Kristallines photovoltaisches Solarmodul
EP1805787A2 (de) * 2004-10-13 2007-07-11 Corning Incorporated Luftdicht verschlossene glasverpackung und fertigungsverfahren
DE102009031972A1 (de) 2009-07-02 2011-01-05 Schott Ag Photovoltaikmodul
CN102951841A (zh) * 2011-08-23 2013-03-06 扬州通和玻璃有限公司 一种太阳能光伏电池用高硼硅玻璃的制备方法

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US4746634A (en) * 1987-05-28 1988-05-24 Corning Glass Works Solarization-resistant glass microsheet
DE4012288C1 (de) * 1990-04-17 1991-07-18 Schott Glaswerke, 6500 Mainz, De
JPH0582822A (ja) * 1991-09-25 1993-04-02 Nippon Electric Glass Co Ltd 太陽電池保護カバー
DE4306004A1 (en) * 1992-03-19 1993-09-23 Horst Hans Juergen Silicate glass suitable for working with short wave solid body lasers - contains iron oxide and opt. vanadium and titanium oxide(s)
DE4230607C1 (de) * 1992-09-12 1994-01-05 Schott Glaswerke Chemisch und thermisch hochbelastbares, mit Wolfram verschmelzbares Borosilikatglas und dessen Verwendung
US5447891A (en) * 1993-09-29 1995-09-05 Ferro Corporation Lead-free glaze or enamel for use on ceramic bodies
FR2728557A1 (fr) 1994-12-27 1996-06-28 Corning France Nouveaux verres et lentilles ophtalmiques
CN1130315C (zh) * 1995-09-22 2003-12-10 株式会社村田制作所 用于高频电路的具有低介电常数的玻璃组合物
JPH0986955A (ja) * 1995-09-29 1997-03-31 Murata Mfg Co Ltd 絶縁体用ガラス組成物、絶縁体ペースト、および厚膜印刷回路
DE19536708C1 (de) * 1995-09-30 1996-10-31 Jenaer Glaswerk Gmbh Zirkon- und lithiumoxidhaltiges Borosilicatglas hoher chemischer Beständigkeit und geringer Viskosität und dessen Verwendung
US5932502A (en) * 1996-04-19 1999-08-03 Guardian Industries Corp. Low transmittance glass
FR2832811B1 (fr) * 2001-11-28 2004-01-30 Saint Gobain Plaque transparente texturee a forte transmission de lumiere
KR100471651B1 (ko) * 2002-01-14 2005-03-08 한국과학기술연구원 저온 소성 유전체 세라믹 조성물 및 이의 제조방법
DE102004027119A1 (de) * 2003-06-06 2004-12-30 Schott Ag UV-Strahlung absorbierendes Glas mit geringer Absorption im sichtbaren Bereich, ein Verfahren zu seiner Herstellung sowie dessen Verwendung
US7045475B2 (en) * 2004-04-28 2006-05-16 Pq Corporation High refractive index glass beads for high retroreflectivity surfaces
CN101066835B (zh) * 2007-06-11 2010-12-08 中国洛阳浮法玻璃集团有限责任公司 太阳能超白压延玻璃组分
IL204034A (en) * 2009-02-24 2015-05-31 Schott Ag Photovoltaic device with central optics
US9371247B2 (en) 2009-05-29 2016-06-21 Corsam Technologies Llc Fusion formable sodium free glass
CN102503123B (zh) * 2011-11-24 2013-08-21 秦皇岛星箭特种玻璃有限公司 空间用抗辐照玻璃盖片的制备方法
GB2509480A (en) * 2012-07-06 2014-07-09 Qioptiq Ltd Radiation stable shield
JP6172445B2 (ja) * 2013-03-08 2017-08-02 日本電気硝子株式会社 カバーガラス

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3499775A (en) * 1966-07-01 1970-03-10 Owens Illinois Inc Ultraviolet-absorbing glass compositions containing cerium and molybdenum oxides
GB1321654A (en) * 1969-09-29 1973-06-27 Gen Electric Glass-to-metal seals
US3843376A (en) * 1971-04-24 1974-10-22 Philips Corp Method of manufacturing a mixture for a borosilicate glass
US4562161A (en) * 1982-02-20 1985-12-31 Schott Glaswerke Optical and ophthalmic glass with refractive indices greater than or equal to 1.56, Abbe numbers greater than or equal to 40 and densities less than or equal to 2.70 g/cm3

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US2657146A (en) * 1951-09-29 1953-10-27 Bausch & Lomb Borosilicate optical glass
US3022181A (en) * 1961-02-01 1962-02-20 Corning Glass Works Glass color filter
US3146120A (en) * 1962-01-11 1964-08-25 American Optical Corp Absorptive glasses
US3404015A (en) * 1965-04-28 1968-10-01 Corning Glass Works Low thermal expansion glasses
US3499776A (en) * 1966-07-13 1970-03-10 Owens Illinois Inc Alkali metal borosilicate glass compositions containing zirconia
US3519446A (en) * 1968-09-19 1970-07-07 Physical Sciences Corp Ceramic material
JPS5632347A (en) * 1979-08-28 1981-04-01 Asahi Glass Co Ltd Glass for tungsten halogen electric bulb
FR2550187B1 (fr) * 1983-08-02 1986-06-06 Corning Glass Works Verres de faible densite et de haut indice de refraction pour applications ophtalmiques et optiques
FR2558152B1 (fr) * 1984-01-13 1992-03-27 Corning Glass Works Verres a usage ophtalmique de faible densite, absorbant les radiations ultraviolettes et ayant une haute transmission dans le visible et lentilles correctrices constituees de ces verres

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3499775A (en) * 1966-07-01 1970-03-10 Owens Illinois Inc Ultraviolet-absorbing glass compositions containing cerium and molybdenum oxides
GB1321654A (en) * 1969-09-29 1973-06-27 Gen Electric Glass-to-metal seals
US3843376A (en) * 1971-04-24 1974-10-22 Philips Corp Method of manufacturing a mixture for a borosilicate glass
US4562161A (en) * 1982-02-20 1985-12-31 Schott Glaswerke Optical and ophthalmic glass with refractive indices greater than or equal to 1.56, Abbe numbers greater than or equal to 40 and densities less than or equal to 2.70 g/cm3

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0505061A3 (en) * 1991-03-22 1993-05-05 Pilkington Plc Borosilicate glass composition
EP0505061A2 (de) * 1991-03-22 1992-09-23 Pilkington Plc Borosilicatglaszusammensetzung
EP0779252A1 (de) 1995-12-08 1997-06-18 Pilkington Plc Strahlungsbeständiges Glas und Glasgegenstände
US5895719A (en) * 1995-12-08 1999-04-20 Pilkington Plc Borosilicate glasses and second surface mirrors thereof
US6180218B1 (en) 1995-12-08 2001-01-30 Pilkington Plc Borosilicate glasses and second surface mirrors thereof
US6207603B1 (en) 1999-02-05 2001-03-27 Corning Incorporated Solar cell cover glass
EP1026130A1 (de) * 1999-02-05 2000-08-09 Corning Incorporated Glas für Abdeckung von Sonnenzellen
US6262358B1 (en) * 1999-02-18 2001-07-17 Sharp Kabushiki Kaisha Solar cell module and solar cell panel using the same
EP1059674A2 (de) * 1999-06-09 2000-12-13 Sharp Kabushiki Kaisha Abgedeckte Solarzelle und Herstellungsverfahren
US6355875B1 (en) * 1999-06-09 2002-03-12 Sharp Kabushiki Kaisha Covered solar cell and manufacturing method thereof
EP1059674A3 (de) * 1999-06-09 2004-01-21 Sharp Kabushiki Kaisha Abgedeckte Solarzelle und Herstellungsverfahren
US8148179B2 (en) 2003-04-16 2012-04-03 Corning Incorporated Hermetically sealed glass package and method of fabrication
EP1805787A2 (de) * 2004-10-13 2007-07-11 Corning Incorporated Luftdicht verschlossene glasverpackung und fertigungsverfahren
EP1805787A4 (de) * 2004-10-13 2011-02-02 Corning Inc Luftdicht verschlossene glasverpackung und fertigungsverfahren
EP1798775A2 (de) * 2005-12-17 2007-06-20 Solarwatt Ag Kristallines photovoltaisches Solarmodul
EP1798775A3 (de) * 2005-12-17 2008-02-20 Solarwatt Ag Kristallines photovoltaisches Solarmodul
DE102009031972A1 (de) 2009-07-02 2011-01-05 Schott Ag Photovoltaikmodul
DE102009031972B4 (de) * 2009-07-02 2013-01-03 Schott Ag Photovoltaikmodul und Verwendung eines Glases für ein Photovoltaikmodul
CN102951841A (zh) * 2011-08-23 2013-03-06 扬州通和玻璃有限公司 一种太阳能光伏电池用高硼硅玻璃的制备方法

Also Published As

Publication number Publication date
KR880003841A (ko) 1988-05-30
GB8623214D0 (en) 1986-10-29
KR950006200B1 (ko) 1995-06-12
EP0261885B1 (de) 1991-01-23
JPH07100616B2 (ja) 1995-11-01
JPS6395138A (ja) 1988-04-26
US5017521A (en) 1991-05-21
DE3767633D1 (de) 1991-02-28

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